TY - JOUR
T1 - Treat-to-target in systemic lupus erythematosus
T2 - advancing towards its implementation
AU - Parra Sánchez, Agner R.
AU - Voskuyl, Alexandre E.
AU - van Vollenhoven, Ronald F.
N1 - Funding Information:
The work of A.R.P.S. is supported by the European Union’s Horizon 2020 research and innovation programme support for the Amsterdam Rheumatology Center for Autoimmune Diseases (ARCAID; grant number 847551).
Funding Information:
R.F.v.V. declares that he has received research support (institutional grants) from BMS, GSK, Lilly and UCB and support for educational programmes from Pfizer and Roche. R.F.v.V. declares that he has also received consulting fees from AbbVie, AstraZeneca, Biogen, Biotest, BMS, Galapagos, Gilead, Janssen, Pfizer, Sanofi, Servier, UCB and Vielabio and personal honoraria as a speaker from AbbVie, Galapagos, GSK, Janssen, Pfizer and UCB. A.E.V. declares that he has received research support (institutional grants) from GSK and UCB, consulting fees from GSK, AstraZeneca and Roche, and personal honoraria as a speaker from GSK. A.R.P.S. declares no competing interests.
Publisher Copyright:
© 2022, Springer Nature Limited.
PY - 2022/3/1
Y1 - 2022/3/1
N2 - The treat-to-target (T2T) concept has improved outcomes for patients with diabetes, hypertension and rheumatoid arthritis. This therapeutic strategy involves choosing a well-defined, relevant target, taking therapeutic steps, evaluating whether the target has been achieved, and taking action if it has not. The T2T principle has been embraced by systemic lupus erythematosus (SLE) experts, but measurable and achievable outcomes, and therapeutic options, are needed to make this approach possible in practice. Considerable evidence has been generated regarding meaningful ‘state’ outcomes for SLE. Low disease activity has been defined and studied, and the most aspirational goal, remission, has been defined by the Definition of Remission in SLE task force. By contrast, current therapeutic options in SLE are limited, and more effective and safer therapies are urgently needed. Fortunately, clinical trial activity in SLE has been unprecedented, and encouraging results have been seen for novel therapies, including biologic and small-molecule agents. Thus, with the expected advent of such treatments, it is likely that sufficiently diverse therapies for SLE will be available in the foreseeable future, allowing the routine implementation of T2T approaches in the care of patients with SLE.
AB - The treat-to-target (T2T) concept has improved outcomes for patients with diabetes, hypertension and rheumatoid arthritis. This therapeutic strategy involves choosing a well-defined, relevant target, taking therapeutic steps, evaluating whether the target has been achieved, and taking action if it has not. The T2T principle has been embraced by systemic lupus erythematosus (SLE) experts, but measurable and achievable outcomes, and therapeutic options, are needed to make this approach possible in practice. Considerable evidence has been generated regarding meaningful ‘state’ outcomes for SLE. Low disease activity has been defined and studied, and the most aspirational goal, remission, has been defined by the Definition of Remission in SLE task force. By contrast, current therapeutic options in SLE are limited, and more effective and safer therapies are urgently needed. Fortunately, clinical trial activity in SLE has been unprecedented, and encouraging results have been seen for novel therapies, including biologic and small-molecule agents. Thus, with the expected advent of such treatments, it is likely that sufficiently diverse therapies for SLE will be available in the foreseeable future, allowing the routine implementation of T2T approaches in the care of patients with SLE.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85122867294&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/35039665
U2 - 10.1038/s41584-021-00739-3
DO - 10.1038/s41584-021-00739-3
M3 - Review article
C2 - 35039665
SN - 1759-4790
VL - 18
SP - 146
EP - 157
JO - Nature Reviews Rheumatology
JF - Nature Reviews Rheumatology
IS - 3
ER -